Contact Heather Lennox | | Data Analyst (Pharmaceutical) - Coleraine - Permanent Are you detail-driven with a passion for quality and compliance? Were recruiting for a Data Reviewer to join a leading pharmaceutical manufacturing environment where precision, collaboration, and continuous improvement are at the heart of everything they do. This is an excellent opportunity for someone with laboratory or pharmaceutical quality experience who enjoys working in a highly regulated environment and wants to be part of a business known for innovation, employee wellbeing and career development. Why apply? Alongside a competitive, negotiable salary, employees benefit from a strong package designed to support both professional growth and personal wellbeing, including: Enhanced annual leave entitlement Healthcare and wellbeing initiatives Pension scheme Life assurance Training and career development opportunities Employee assistance programme Modern working environment Health & wellbeing activities Recognition and reward initiatives The Role Working within the Quality Control Laboratory, you will play a key role in ensuring all laboratory data, testing, and documentation meet strict regulatory and GMP standards. Reviewing analytical data for products, materials, validation, and stability studies Reviewing equipment calibration and verification records Compiling and reviewing laboratory testing instructions, specifications, and SOPs Preparing validation protocols and reviewing associated reports Coordinating calibration schedules for laboratory equipment Preparing and reviewing technical reports and regulatory submission documentation Supporting qualification activities for facilities and equipment when required Maintaining compliance with cGMP, FDA, MHRA, and internal quality standards Supporting a safe working environment through adherence to EHS procedures and participation in inspections and risk assessments Working flexibly to support departmental and business objectives Criteria: Degree in Chemistry or a related scientific discipline Experience working within a GLP/GMP regulated environment Knowledge of pharmaceutical regulatory requirements, particularly FDA or MHRA standards Strong attention to detail and organisational skills Comfortable working independently and collaboratively within strict regulatory frameworks Proficient in Microsoft Office and computer-based systems Self-motivated with a proactive approach to problem solving If this sounds like the next step in your career, wed love to hear from you! Even if you dont meet every listed requirement, we encourage you to apply we may have other suitable roles for you. Apply online, email or call Heather on to find out more. Riada Resourcing is an equal opportunities employer. Skills: Admin Analyst ADZN1_NI